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Clinical Trial Summary

In this study, eligible subjects with moderate to severe nasolabial folds will be treated with Princess® FILLER Lidocaine and will return for follow-up assessments 2, 4, 24 and 36 weeks after the treatment. A Touch-up treatment may be done at Week 2, if deemed appropriate by the investigator


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03611491
Study type Interventional
Source Croma-Pharma GmbH
Contact
Status Completed
Phase N/A
Start date September 20, 2017
Completion date November 19, 2018

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